产品货号：
JN1985
中文名称：
重组人β-脲基丙酸酶
英文名称：
Recombinant Human beta-Ureidopropionase
产品规格：
10μg|50μg|500μg|1mg
发货周期：
1～3天
产品价格：
询价
本品由我们的大肠杆菌表达系统制备而成，目的基因编码的Met1-Glu384在C端含有His标签。
β-Ureidopropionase质量控制：＞95%(还原性SDS-PAGE)
β-Ureidopropionase制剂：液体
β-Ureidopropionase保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于β-Ureidopropionase：
β-Ureidopropionase is a cytoplasmic protein which belongs to the CN hydrolase family of BUP subfamily. β-Ureidopropionase binds one zinc ion per subunit, catalyzes the last step in the pyrimidine degradation pathway. β-Ureidopropionase can convert N-carbamyl-beta-aminoisobutyric acid and N-carbamyl-beta-alanine to beta-aminoisobutyric acid and beta-alanine, ammonia and carbon dioxide, respectively. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta aminoisobutyric acid, respectively. Defects in β-Ureidopropionase are the cause of β-Ureidopropionase deficiency that is characterized by muscular hypotonia, dystonic movements, scoliosis, microcephaly and severe developmental delay.
相关搜索：重组人β-脲基丙酸酶，Recombinant Human beta-Ureidopropionase
β-Ureidopropionase质量控制：＞95%(还原性SDS-PAGE)
β-Ureidopropionase制剂：液体
β-Ureidopropionase保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于β-Ureidopropionase：
β-Ureidopropionase is a cytoplasmic protein which belongs to the CN hydrolase family of BUP subfamily. β-Ureidopropionase binds one zinc ion per subunit, catalyzes the last step in the pyrimidine degradation pathway. β-Ureidopropionase can convert N-carbamyl-beta-aminoisobutyric acid and N-carbamyl-beta-alanine to beta-aminoisobutyric acid and beta-alanine, ammonia and carbon dioxide, respectively. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta aminoisobutyric acid, respectively. Defects in β-Ureidopropionase are the cause of β-Ureidopropionase deficiency that is characterized by muscular hypotonia, dystonic movements, scoliosis, microcephaly and severe developmental delay.
相关搜索：重组人β-脲基丙酸酶，Recombinant Human beta-Ureidopropionase